A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590458



Internal ID20963529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92754344..92755362hg38UCSC Ensembl
chr11:92487510..92488528hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222663
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590458
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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